Intracranial neuromuscular choristoma: Report of a case with literature review

被引:4
|
作者
Coli, Antonella [1 ]
Novello, Mariangela [1 ]
Tamburrini, Gianpiero [2 ]
Antonelli, Manila [3 ]
Giangaspero, Felice [3 ,4 ]
Lauriola, Libero [1 ]
机构
[1] Catholic Univ, Dept Anat Pathol, Rome, Italy
[2] Catholic Univ, Dept Pediat Neurosurg, Rome, Italy
[3] Sapienza Univ Rome, Dept Radiol Oncol & Anatomopathol Sci, Rome, Italy
[4] IRCCS Neuromed, Rome, Italy
关键词
choristoma; cranial nerves; neural crest; neuromuscular hamartoma; skeletal muscle; INTERNAL AUDITORY MEATUS; BENIGN TRITON TUMOR; NERVE RHABDOMYOMA; TRIGEMINAL NERVE; STRIATED-MUSCLE; SCHWANN-CELLS; HAMARTOMA; CHILD; MULTIPOTENCY; FIBROMATOSIS;
D O I
10.1111/neup.12368
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Neuromuscular choristoma (NMC), also called neuromuscular hamartoma or nerve rhabdomyoma, is a rare lesion of the spinal and cranial nerves composed of skeletal muscle intimately associated with nerve fibers. Its origin has not been precisely clarified and a malformative event, resulting from aberrant differentiation or a true neoplastic growth, have been proposed by authors. We hereby present a cerebellopontine angle NMC enlarging the eighth cranial nerve in a 3-year-old child, that histologically appeared composed of a large amount of striated muscle mixed with nerve fibers. We also provide a review of the intracranial NMC cases reported in the literature and an analysis of proposed hypotheses to explain the presence of muscle cells in nerve trunks.
引用
收藏
页码:341 / 345
页数:5
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